| Weight | 131.178 g/mol |
|---|---|
| Formula | C9H9N |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
6-Methylindole (3420-02-8)
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- A biosynthetic approach to the structure of eumelanins. The isolation of oligomers from 5,6-dihydroxy-1-methylindole. (Tetrahedron, 1986)
- Melanin. 2. Electrochemical study of the oxidation of .alpha.-methyldopa and 5,6-dihydroxy-2-methylindole (Journal of Organic Chemistry, 1980)
- The mycotoxin verruculogen: a 6-O-methylindole. (Journal of Agricultural and Food Chemistry, 1973)
- Reaction of 4,6-Dimethoxy-3-methylindole With Aromatic Aldehydes: a Simple Synthesis of Calix[3]indoles (Australian Journal of Chemistry, 1996)
- Metal template reactions. XX. Macrocyclic metal complexes derived from 4,6-Dimethoxy-3-methylindole-2,7-dicarbaldehyde and some primary diamines with additional nitrogen donor atoms (Australian Journal of Chemistry, 1983)
- Efficient Synthesis of Indoloquinone Derivations by Several Oxidative Derivatib\ves of 6-Methylindole (Heterocycles, 1987)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CC2=C(C=C1)C=CN2
-
InChIKeyONYNOPPOVKYGRS-UHFFFAOYSA-N
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